中国药学(英文版)
中國藥學(英文版)
중국약학(영문판)
JOURNAL OF CHINESE PHARMACEUTICAL SCIENCES
2007年
1期
51-56
,共6页
朱静%杨照罡%陈晓梅%孙葭北%古丽斯坦·阿吾提%张烜%张强
硃靜%楊照罡%陳曉梅%孫葭北%古麗斯坦·阿吾提%張烜%張彊
주정%양조강%진효매%손가북%고려사탄·아오제%장훤%장강
槲皮素%PVP%固体分散体%溶出率
槲皮素%PVP%固體分散體%溶齣率
곡피소%PVP%고체분산체%용출솔
Quercetin%Polyvinylpyrrolidone (PVP)%Solid dispersion%Dissolution rate
目的 用溶剂法制备槲皮素-PVP固体分散体并考察其溶出特性并对物相进行鉴定.方法 采用溶剂法制备槲皮素-PVP固体分散体,通过溶出实验对槲皮素溶出率的测定研究固体分散体的溶出性质,利用差热分析(Differential scanning calorimetry,DSC)、红外光谱分析(Infrared spectroscopy,IR)、粉末X衍射(X-ray powder diffractometry,PXRD)、扫描电镜(Scanning electron microscopy,SEM)等方法对其进行物相鉴定.结果 槲皮素-PVP固体分散体的溶出速率相对其物理混合物有了明显的改善;溶解实验显示固体分散体中槲皮素的溶解度有了显著的提高;热差分析及粉末X衍射结果表明固体分散体中槲皮素呈非结晶形式;扫描电镜下固体分散体中无槲皮素晶体.结论 采用溶剂法制备槲皮素-PVP固体分散体可显著提高槲皮素的溶解度及溶出速度.
目的 用溶劑法製備槲皮素-PVP固體分散體併攷察其溶齣特性併對物相進行鑒定.方法 採用溶劑法製備槲皮素-PVP固體分散體,通過溶齣實驗對槲皮素溶齣率的測定研究固體分散體的溶齣性質,利用差熱分析(Differential scanning calorimetry,DSC)、紅外光譜分析(Infrared spectroscopy,IR)、粉末X衍射(X-ray powder diffractometry,PXRD)、掃描電鏡(Scanning electron microscopy,SEM)等方法對其進行物相鑒定.結果 槲皮素-PVP固體分散體的溶齣速率相對其物理混閤物有瞭明顯的改善;溶解實驗顯示固體分散體中槲皮素的溶解度有瞭顯著的提高;熱差分析及粉末X衍射結果錶明固體分散體中槲皮素呈非結晶形式;掃描電鏡下固體分散體中無槲皮素晶體.結論 採用溶劑法製備槲皮素-PVP固體分散體可顯著提高槲皮素的溶解度及溶齣速度.
목적 용용제법제비곡피소-PVP고체분산체병고찰기용출특성병대물상진행감정.방법 채용용제법제비곡피소-PVP고체분산체,통과용출실험대곡피소용출솔적측정연구고체분산체적용출성질,이용차열분석(Differential scanning calorimetry,DSC)、홍외광보분석(Infrared spectroscopy,IR)、분말X연사(X-ray powder diffractometry,PXRD)、소묘전경(Scanning electron microscopy,SEM)등방법대기진행물상감정.결과 곡피소-PVP고체분산체적용출속솔상대기물리혼합물유료명현적개선;용해실험현시고체분산체중곡피소적용해도유료현저적제고;열차분석급분말X연사결과표명고체분산체중곡피소정비결정형식;소묘전경하고체분산체중무곡피소정체.결론 채용용제법제비곡피소-PVP고체분산체가현저제고곡피소적용해도급용출속도.
Aim The objective of this study was to prepare and characterize quercetin-polyvinylpyrrolidone (Qurc-PVP)solid dispersion with the intention of improving its dissolution properties. Methods Qurc-PVP sclid dispersion was prepared by solvent method. The release rate of quercetin was determined from dissolution studies and the physicochemical properties of solid dispersion were investigated by differential scanning calorimetry (DSC), infrared spectroscopy (IR), powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM). Results The results showed that the dissolution rate of quercetin was significantly improved by solid dispersion compared to that of the pure drug and physical mixture. Solubility studies revealed a markedly increase in the solubility of quercetin. The results of DSC and PXRD showed that the quercetin in solid dispersion was amorphous form. From SEM analysis, there was no quercetin crystal observed in the solid dispersions.Conclusion The solubility and dissolution of quercetin were improved by solid dispersion technique.